US7374742B2ExpiredUtilityA1
Direct sulfur recovery system
Est. expiryDec 19, 2023(expired)· nominal 20-yr term from priority
C01B 2203/84Y02E20/16B01D 53/1456C01B 3/52C01B 2203/0455C10L 3/102C01B 2203/0283Y02E20/18C01B 17/0404C01B 3/12C10L 3/10C10K 1/34C01B 17/0408C01B 2203/0485
79
PatentIndex Score
22
Cited by
11
References
29
Claims
Abstract
The present invention provides a method for removing sulfur species from a gas stream without the use of a sulfur species removal process, such as an amine scrub. The sulfur species are removed by directly subjecting the gas stream to a sulfur recovery process, such as a Claus or sub-dewpoint Claus process at high pressure and moderate temperatures, wherein the sulfur recovery process comprises a catalyst which does not comprise activated carbon.
Claims
exact text as granted — not AI-modified1. A method for producing a sweet gas stream from a sour gas stream, wherein the sweet gas stream comprises a decreased mole fraction of a sulfur species and an increased mole fraction of a fuel species in relation to the sour gas stream, said method comprising:
(a) subjecting the sour gas stream to a sulfur recovery process, thus producing a sweet gas stream, without first subjecting the sour gas stream to a sulfur species removal process, said sulfur recovery process comprising a catalyst which does not comprise activated carbon, wherein said sulfur recovery process is a sub-dewpoint Claus process conducted at a pressure of between 10 atm and 110 atm and at a temperature of between about 300° F. and about 500° F., wherein the sulfur recovery process converts H 2 S to elemental sulfur.
2. The method according to claim 1 , wherein said sour gas stream is not subjected to a change in pressure prior to step (a).
3. The method according to claim 1 , wherein said sour gas stream is not subjected to a change in temperature prior to step (a).
4. The method according to claim 1 , wherein said sulfur recovery process is conducted at a pressure of between about 20 atm and 50 atm.
5. The method according to claim 1 , wherein said sulfur recovery process is conducted at a temperature of between about 300° F. and about 400° F.
6. The method according to claim 1 , wherein the sour gas stream comprises natural gas.
7. The method according to claim 1 , wherein the sour gas stream comprises synthesis gas.
8. The method according to claim 1 , wherein the sour gas stream comprises refinery fuel gas.
9. The method according to claim 1 , wherein the sulfur species mole fraction in said sour gas stream is 10% or less.
10. The method according to claim 1 , wherein said sulfur species removal process is selected from amine scrubbing, solvent absorption, adsorption, electrochemical oxidation, and membrane treatment.
11. The method according to claim 1 , wherein, in addition to the sour gas stream, a gas selected from air, O 2 , SO 2 and combinations thereof, is introduced into said sulfur recovery process.
12. The method according to claim 1 , wherein said elemental sulfur is a liquid.
13. The method according to claim 12 , wherein said elemental sulfur collects on said catalyst, and said method further comprises regenerating said catalyst.
14. The method according to claim 13 , wherein said regenerating comprises:
a) depressurizing said sulfur recovery process;
b) heating said catalyst;
c) converting said solid sulfur and said liquid sulfur into sulfur vapor;
d) removing said sulfur vapor from said sulfur recovery system; and
e) cooling said catalyst.
15. The method according to claim 1 , wherein said sulfur recovery process decreases the mole fraction of sulfur species in the sour gas stream by at least about 70%.
16. The method according to claim 1 , wherein said sulfur recovery process decreases the mole fraction of sulfur species in the sour gas stream by at least about 98%.
17. The method according to claim 1 , wherein said sulfur recovery process increases the CO 2 mole fraction in said sour gas stream.
18. The method according to claim 1 , wherein a property of said sour gas stream is altered, said property selected from humidity, temperature, pressure, and combinations thereof.
19. The method according to claim 1 , further comprising subjecting said sour gas stream to a steam generation process.
20. The method according to claim 1 , further comprising subjecting said sweet gas stream to a steam generation process.
21. The method according to claim 1 , further comprising removing particulate material from said sour gas stream.
22. The method according to claim 1 , further comprising removing particulate material from said sweet gas stream.
23. The method according to claim 1 , further comprising contacting said sweet gas stream with an adsorbent filter to capture residual particles.
24. The method according to claim 23 , wherein said adsorbent filter is selected from activated carbon, coal, and coke.
25. The method according to claim 23 , further comprising regenerating said adsorbent filter.
26. The method according to claim 25 , wherein said regenerating comprises:
a) using steam or clean gas stream to absorb said residual particles; and
b) subjecting the product of step (a) to said sulfur recovery process.
27. The method according to claim 1 , further comprising subjecting said sweet gas stream to a CO 2 recovery process, thus producing a low CO 2 sweet gas stream.
28. The method according to claim 1 , further comprising washing said sweet gas stream with water.
29. The method according to claim 1 , further comprising separating said elemental sulfur by using an apparatus selected from a knock-out drum, coalescer, and filter.Cited by (0)
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